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Huber‐Gedert <i>et al.</i>, “Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad,” <i>Chemistry – A European Journal</i>, vol. 27, no. 38, pp. 9905–9918, 2021, doi: <a href=\"https://doi.org/10.1002/chem.202100766\">10.1002/chem.202100766</a>.","chicago":"Huber‐Gedert, Marina, Michał Nowakowski, Ahmet Kertmen, Lukas Burkhardt, Natalia Lindner, Roland Schoch, Regine Herbst‐Irmer, et al. “Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad.” <i>Chemistry – A European Journal</i> 27, no. 38 (2021): 9905–18. <a href=\"https://doi.org/10.1002/chem.202100766\">https://doi.org/10.1002/chem.202100766</a>.","ama":"Huber‐Gedert M, Nowakowski M, Kertmen A, et al. Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad. <i>Chemistry – A European Journal</i>. 2021;27(38):9905-9918. doi:<a href=\"https://doi.org/10.1002/chem.202100766\">10.1002/chem.202100766</a>","apa":"Huber‐Gedert, M., Nowakowski, M., Kertmen, A., Burkhardt, L., Lindner, N., Schoch, R., Herbst‐Irmer, R., Neuba, A., Schmitz, L., Choi, T., Kubicki, J., Gawelda, W., &#38; Bauer, M. (2021). Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad. <i>Chemistry – A European Journal</i>, <i>27</i>(38), 9905–9918. <a href=\"https://doi.org/10.1002/chem.202100766\">https://doi.org/10.1002/chem.202100766</a>","mla":"Huber‐Gedert, Marina, et al. “Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad.” <i>Chemistry – A European Journal</i>, vol. 27, no. 38, Wiley, 2021, pp. 9905–18, doi:<a href=\"https://doi.org/10.1002/chem.202100766\">10.1002/chem.202100766</a>.","bibtex":"@article{Huber‐Gedert_Nowakowski_Kertmen_Burkhardt_Lindner_Schoch_Herbst‐Irmer_Neuba_Schmitz_Choi_et al._2021, title={Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad}, volume={27}, DOI={<a href=\"https://doi.org/10.1002/chem.202100766\">10.1002/chem.202100766</a>}, number={38}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Huber‐Gedert, Marina and Nowakowski, Michał and Kertmen, Ahmet and Burkhardt, Lukas and Lindner, Natalia and Schoch, Roland and Herbst‐Irmer, Regine and Neuba, Adam and Schmitz, Lennart and Choi, Tae‐Kyu and et al.}, year={2021}, pages={9905–9918} }","short":"M. Huber‐Gedert, M. Nowakowski, A. Kertmen, L. Burkhardt, N. Lindner, R. Schoch, R. Herbst‐Irmer, A. Neuba, L. Schmitz, T. Choi, J. Kubicki, W. Gawelda, M. Bauer, Chemistry – A European Journal 27 (2021) 9905–9918."},"year":"2021","issue":"38","publication_identifier":{"issn":["0947-6539","1521-3765"]},"publication_status":"published"},{"status":"public","publication":"Chemistry – A European Journal","type":"journal_article","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"language":[{"iso":"eng"}],"_id":"41322","user_id":"78878","year":"2021","page":"17220-17229","intvolume":"        27","citation":{"ama":"Panyam PKR, Atwi B, Ziegler F, et al. Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes. <i>Chemistry – A European Journal</i>. 2021;27(68):17220-17229. doi:<a href=\"https://doi.org/10.1002/chem.202103099\">10.1002/chem.202103099</a>","ieee":"P. K. R. Panyam <i>et al.</i>, “Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes,” <i>Chemistry – A European Journal</i>, vol. 27, no. 68, pp. 17220–17229, 2021, doi: <a href=\"https://doi.org/10.1002/chem.202103099\">10.1002/chem.202103099</a>.","chicago":"Panyam, Pradeep K. R., Boshra Atwi, Felix Ziegler, Wolfgang Frey, Michal Nowakowski, Matthias Bauer, and Michael R. Buchmeiser. “Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes.” <i>Chemistry – A European Journal</i> 27, no. 68 (2021): 17220–29. <a href=\"https://doi.org/10.1002/chem.202103099\">https://doi.org/10.1002/chem.202103099</a>.","apa":"Panyam, P. K. R., Atwi, B., Ziegler, F., Frey, W., Nowakowski, M., Bauer, M., &#38; Buchmeiser, M. R. (2021). Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes. <i>Chemistry – A European Journal</i>, <i>27</i>(68), 17220–17229. <a href=\"https://doi.org/10.1002/chem.202103099\">https://doi.org/10.1002/chem.202103099</a>","short":"P.K.R. Panyam, B. Atwi, F. Ziegler, W. Frey, M. Nowakowski, M. Bauer, M.R. Buchmeiser, Chemistry – A European Journal 27 (2021) 17220–17229.","mla":"Panyam, Pradeep K. R., et al. “Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes.” <i>Chemistry – A European Journal</i>, vol. 27, no. 68, Wiley, 2021, pp. 17220–29, doi:<a href=\"https://doi.org/10.1002/chem.202103099\">10.1002/chem.202103099</a>.","bibtex":"@article{Panyam_Atwi_Ziegler_Frey_Nowakowski_Bauer_Buchmeiser_2021, title={Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes}, volume={27}, DOI={<a href=\"https://doi.org/10.1002/chem.202103099\">10.1002/chem.202103099</a>}, number={68}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Panyam, Pradeep K. R. and Atwi, Boshra and Ziegler, Felix and Frey, Wolfgang and Nowakowski, Michal and Bauer, Matthias and Buchmeiser, Michael R.}, year={2021}, pages={17220–17229} }"},"publication_identifier":{"issn":["0947-6539","1521-3765"]},"publication_status":"published","issue":"68","title":"Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes","doi":"10.1002/chem.202103099","publisher":"Wiley","date_updated":"2023-02-01T08:51:03Z","volume":27,"date_created":"2023-01-31T22:50:03Z","author":[{"last_name":"Panyam","full_name":"Panyam, Pradeep K. R.","first_name":"Pradeep K. R."},{"full_name":"Atwi, Boshra","last_name":"Atwi","first_name":"Boshra"},{"last_name":"Ziegler","full_name":"Ziegler, Felix","first_name":"Felix"},{"first_name":"Wolfgang","full_name":"Frey, Wolfgang","last_name":"Frey"},{"last_name":"Nowakowski","full_name":"Nowakowski, Michal","first_name":"Michal"},{"full_name":"Bauer, Matthias","last_name":"Bauer","first_name":"Matthias"},{"last_name":"Buchmeiser","full_name":"Buchmeiser, Michael R.","first_name":"Michael R."}]},{"keyword":["Inorganic Chemistry","Organic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"_id":"41324","user_id":"78878","status":"public","publication":"Organometallics","type":"journal_article","title":"Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations","doi":"10.1021/acs.organomet.1c00216","date_updated":"2023-02-01T08:50:56Z","publisher":"American Chemical Society (ACS)","volume":40,"author":[{"first_name":"Sarah","full_name":"Maier, Sarah","last_name":"Maier"},{"last_name":"Cronin","full_name":"Cronin, Steve P.","first_name":"Steve P."},{"full_name":"Vu Dinh, Manh-Anh","last_name":"Vu Dinh","first_name":"Manh-Anh"},{"full_name":"Li, Zheng","last_name":"Li","first_name":"Zheng"},{"first_name":"Michael","last_name":"Dyballa","full_name":"Dyballa, Michael"},{"last_name":"Nowakowski","full_name":"Nowakowski, Michal","first_name":"Michal"},{"full_name":"Bauer, Matthias","last_name":"Bauer","first_name":"Matthias"},{"last_name":"Estes","full_name":"Estes, Deven P.","first_name":"Deven P."}],"date_created":"2023-01-31T22:50:43Z","year":"2021","intvolume":"        40","page":"1751-1757","citation":{"apa":"Maier, S., Cronin, S. P., Vu Dinh, M.-A., Li, Z., Dyballa, M., Nowakowski, M., Bauer, M., &#38; Estes, D. P. (2021). Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations. <i>Organometallics</i>, <i>40</i>(11), 1751–1757. <a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">https://doi.org/10.1021/acs.organomet.1c00216</a>","short":"S. Maier, S.P. Cronin, M.-A. Vu Dinh, Z. Li, M. Dyballa, M. Nowakowski, M. Bauer, D.P. Estes, Organometallics 40 (2021) 1751–1757.","bibtex":"@article{Maier_Cronin_Vu Dinh_Li_Dyballa_Nowakowski_Bauer_Estes_2021, title={Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations}, volume={40}, DOI={<a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">10.1021/acs.organomet.1c00216</a>}, number={11}, journal={Organometallics}, publisher={American Chemical Society (ACS)}, author={Maier, Sarah and Cronin, Steve P. and Vu Dinh, Manh-Anh and Li, Zheng and Dyballa, Michael and Nowakowski, Michal and Bauer, Matthias and Estes, Deven P.}, year={2021}, pages={1751–1757} }","mla":"Maier, Sarah, et al. “Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations.” <i>Organometallics</i>, vol. 40, no. 11, American Chemical Society (ACS), 2021, pp. 1751–57, doi:<a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">10.1021/acs.organomet.1c00216</a>.","ama":"Maier S, Cronin SP, Vu Dinh M-A, et al. Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations. <i>Organometallics</i>. 2021;40(11):1751-1757. doi:<a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">10.1021/acs.organomet.1c00216</a>","ieee":"S. Maier <i>et al.</i>, “Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations,” <i>Organometallics</i>, vol. 40, no. 11, pp. 1751–1757, 2021, doi: <a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">10.1021/acs.organomet.1c00216</a>.","chicago":"Maier, Sarah, Steve P. Cronin, Manh-Anh Vu Dinh, Zheng Li, Michael Dyballa, Michal Nowakowski, Matthias Bauer, and Deven P. Estes. “Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations.” <i>Organometallics</i> 40, no. 11 (2021): 1751–57. <a href=\"https://doi.org/10.1021/acs.organomet.1c00216\">https://doi.org/10.1021/acs.organomet.1c00216</a>."},"publication_identifier":{"issn":["0276-7333","1520-6041"]},"publication_status":"published","issue":"11"},{"date_updated":"2023-01-27T16:32:22Z","publisher":"Royal Society of Chemistry (RSC)","volume":10,"date_created":"2023-01-27T16:20:26Z","author":[{"full_name":"Kossmann, Janina","last_name":"Kossmann","first_name":"Janina"},{"last_name":"Ortíz Sánchez-Manjavacas","full_name":"Ortíz Sánchez-Manjavacas, María Luz","first_name":"María Luz"},{"first_name":"Hannes","last_name":"Zschiesche","full_name":"Zschiesche, Hannes"},{"first_name":"Nadezda V.","full_name":"Tarakina, Nadezda V.","last_name":"Tarakina"},{"first_name":"Markus","full_name":"Antonietti, Markus","last_name":"Antonietti"},{"last_name":"Albero","full_name":"Albero, Josep","first_name":"Josep"},{"first_name":"Nieves","full_name":"Lopez Salas, Nieves","id":"98120","orcid":"https://orcid.org/0000-0002-8438-9548","last_name":"Lopez Salas"}],"title":"Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction","doi":"10.1039/d1ta09459a","publication_identifier":{"issn":["2050-7488","2050-7496"]},"publication_status":"published","issue":"11","year":"2021","page":"6107-6114","intvolume":"        10","citation":{"apa":"Kossmann, J., Ortíz Sánchez-Manjavacas, M. L., Zschiesche, H., Tarakina, N. V., Antonietti, M., Albero, J., &#38; Lopez Salas, N. (2021). Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction. <i>Journal of Materials Chemistry A</i>, <i>10</i>(11), 6107–6114. <a href=\"https://doi.org/10.1039/d1ta09459a\">https://doi.org/10.1039/d1ta09459a</a>","mla":"Kossmann, Janina, et al. “Cu<sup>II</sup>/Cu<sup>I</sup> Decorated N-Doped Carbonaceous Electrocatalysts for the Oxygen Reduction Reaction.” <i>Journal of Materials Chemistry A</i>, vol. 10, no. 11, Royal Society of Chemistry (RSC), 2021, pp. 6107–14, doi:<a href=\"https://doi.org/10.1039/d1ta09459a\">10.1039/d1ta09459a</a>.","short":"J. Kossmann, M.L. Ortíz Sánchez-Manjavacas, H. Zschiesche, N.V. Tarakina, M. Antonietti, J. Albero, N. Lopez Salas, Journal of Materials Chemistry A 10 (2021) 6107–6114.","bibtex":"@article{Kossmann_Ortíz Sánchez-Manjavacas_Zschiesche_Tarakina_Antonietti_Albero_Lopez Salas_2021, title={Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction}, volume={10}, DOI={<a href=\"https://doi.org/10.1039/d1ta09459a\">10.1039/d1ta09459a</a>}, number={11}, journal={Journal of Materials Chemistry A}, publisher={Royal Society of Chemistry (RSC)}, author={Kossmann, Janina and Ortíz Sánchez-Manjavacas, María Luz and Zschiesche, Hannes and Tarakina, Nadezda V. and Antonietti, Markus and Albero, Josep and Lopez Salas, Nieves}, year={2021}, pages={6107–6114} }","ama":"Kossmann J, Ortíz Sánchez-Manjavacas ML, Zschiesche H, et al. Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction. <i>Journal of Materials Chemistry A</i>. 2021;10(11):6107-6114. doi:<a href=\"https://doi.org/10.1039/d1ta09459a\">10.1039/d1ta09459a</a>","ieee":"J. Kossmann <i>et al.</i>, “Cu<sup>II</sup>/Cu<sup>I</sup> decorated N-doped carbonaceous electrocatalysts for the oxygen reduction reaction,” <i>Journal of Materials Chemistry A</i>, vol. 10, no. 11, pp. 6107–6114, 2021, doi: <a href=\"https://doi.org/10.1039/d1ta09459a\">10.1039/d1ta09459a</a>.","chicago":"Kossmann, Janina, María Luz Ortíz Sánchez-Manjavacas, Hannes Zschiesche, Nadezda V. Tarakina, Markus Antonietti, Josep Albero, and Nieves Lopez Salas. “Cu<sup>II</sup>/Cu<sup>I</sup> Decorated N-Doped Carbonaceous Electrocatalysts for the Oxygen Reduction Reaction.” <i>Journal of Materials Chemistry A</i> 10, no. 11 (2021): 6107–14. <a href=\"https://doi.org/10.1039/d1ta09459a\">https://doi.org/10.1039/d1ta09459a</a>."},"_id":"40570","user_id":"98120","keyword":["General Materials Science","Renewable Energy","Sustainability and the Environment","General Chemistry"],"language":[{"iso":"eng"}],"publication":"Journal of Materials Chemistry A","type":"journal_article","abstract":[{"text":"<jats:p>Copper- and nitrogen-doped carbonaceous materials, obtained by a simple synthetic procedure are highly efficient and fast catalysts for the oxygen reduction reaction. It is shown, that Cu(<jats:sc>i</jats:sc>) containing materials perform with faster reaction kinetics.</jats:p>","lang":"eng"}],"status":"public"},{"user_id":"98120","_id":"40569","language":[{"iso":"eng"}],"keyword":["Colloid and Surface Chemistry","Surfaces","Coatings and Films","Biomaterials","Electronic","Optical and Magnetic Materials"],"publication":"Journal of Colloid and Interface Science","type":"journal_article","status":"public","volume":602,"date_created":"2023-01-27T16:20:20Z","author":[{"first_name":"Janina","last_name":"Kossmann","full_name":"Kossmann, Janina"},{"full_name":"Rothe, Regina","last_name":"Rothe","first_name":"Regina"},{"first_name":"Tobias","last_name":"Heil","full_name":"Heil, Tobias"},{"first_name":"Markus","full_name":"Antonietti, Markus","last_name":"Antonietti"},{"first_name":"Nieves","last_name":"Lopez Salas","orcid":"https://orcid.org/0000-0002-8438-9548","full_name":"Lopez Salas, Nieves","id":"98120"}],"publisher":"Elsevier BV","date_updated":"2023-01-27T16:32:42Z","doi":"10.1016/j.jcis.2021.06.012","title":"Ultrahigh water sorption on highly nitrogen doped carbonaceous materials derived from uric acid","publication_identifier":{"issn":["0021-9797"]},"publication_status":"published","intvolume":"       602","page":"880-888","citation":{"chicago":"Kossmann, Janina, Regina Rothe, Tobias Heil, Markus Antonietti, and Nieves Lopez Salas. “Ultrahigh Water Sorption on Highly Nitrogen Doped Carbonaceous Materials Derived from Uric Acid.” <i>Journal of Colloid and Interface Science</i> 602 (2021): 880–88. <a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">https://doi.org/10.1016/j.jcis.2021.06.012</a>.","ieee":"J. Kossmann, R. Rothe, T. Heil, M. Antonietti, and N. Lopez Salas, “Ultrahigh water sorption on highly nitrogen doped carbonaceous materials derived from uric acid,” <i>Journal of Colloid and Interface Science</i>, vol. 602, pp. 880–888, 2021, doi: <a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">10.1016/j.jcis.2021.06.012</a>.","ama":"Kossmann J, Rothe R, Heil T, Antonietti M, Lopez Salas N. Ultrahigh water sorption on highly nitrogen doped carbonaceous materials derived from uric acid. <i>Journal of Colloid and Interface Science</i>. 2021;602:880-888. doi:<a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">10.1016/j.jcis.2021.06.012</a>","apa":"Kossmann, J., Rothe, R., Heil, T., Antonietti, M., &#38; Lopez Salas, N. (2021). Ultrahigh water sorption on highly nitrogen doped carbonaceous materials derived from uric acid. <i>Journal of Colloid and Interface Science</i>, <i>602</i>, 880–888. <a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">https://doi.org/10.1016/j.jcis.2021.06.012</a>","mla":"Kossmann, Janina, et al. “Ultrahigh Water Sorption on Highly Nitrogen Doped Carbonaceous Materials Derived from Uric Acid.” <i>Journal of Colloid and Interface Science</i>, vol. 602, Elsevier BV, 2021, pp. 880–88, doi:<a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">10.1016/j.jcis.2021.06.012</a>.","short":"J. Kossmann, R. Rothe, T. Heil, M. Antonietti, N. Lopez Salas, Journal of Colloid and Interface Science 602 (2021) 880–888.","bibtex":"@article{Kossmann_Rothe_Heil_Antonietti_Lopez Salas_2021, title={Ultrahigh water sorption on highly nitrogen doped carbonaceous materials derived from uric acid}, volume={602}, DOI={<a href=\"https://doi.org/10.1016/j.jcis.2021.06.012\">10.1016/j.jcis.2021.06.012</a>}, journal={Journal of Colloid and Interface Science}, publisher={Elsevier BV}, author={Kossmann, Janina and Rothe, Regina and Heil, Tobias and Antonietti, Markus and Lopez Salas, Nieves}, year={2021}, pages={880–888} }"},"year":"2021"},{"title":"Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation","publisher":"American Chemical Society (ACS)","date_created":"2023-01-30T16:49:18Z","year":"2021","issue":"27","keyword":["Surfaces","Coatings and Films","Physical and Theoretical Chemistry","General Energy","Electronic","Optical and Magnetic Materials"],"language":[{"iso":"eng"}],"abstract":[{"lang":"eng","text":"Homogeneous catalysts immobilized on metal oxides often have different catalytic properties than in homogeneous solution. This can be either activating or deactivating and is often attributed to interactions of catalyst species with the metal oxide surface. However, few studies have ever demonstrated the effect that close associations of active sites with surfaces have on the catalytic activity. In this paper, we immobilize H2Ru(PPh3)2(Ph2P)2N–C3H6–Si(OEt)3 (3) on SiO2, Al2O3, and ZnO and interrogate the relationship to the surface using IR, MAS NMR, 1H–31P HETCOR, and XAS spectroscopies. We found that while there are close contacts between the P atoms of the complex and all three metal oxide surfaces, the Ru–H bond only reacts with oxygen bridges on SiO2 and Al2O3, forming new Ru–O bonds. In contrast, complex 3 stays intact on ZnO. Comparison of the catalytic activities of our immobilized species for CO2 hydrogenation to ethyl formate showed that Lewis acidic metal oxides activate, rather than deactivate, complex 3 in the order Al2O3 > ZnO > SiO2. The Lewis acidic sites on the metal oxide surfaces most likely increase the productivity by increasing the rate of esterification of formate intermediates."}],"publication":"The Journal of Physical Chemistry C","doi":"10.1021/acs.jpcc.1c02074","date_updated":"2023-01-31T08:06:00Z","author":[{"last_name":"Nguyen","full_name":"Nguyen, Hoang-Huy","first_name":"Hoang-Huy"},{"first_name":"Zheng","full_name":"Li, Zheng","last_name":"Li"},{"full_name":"Enenkel, Toni","last_name":"Enenkel","first_name":"Toni"},{"full_name":"Hildebrand, Joachim","last_name":"Hildebrand","first_name":"Joachim"},{"orcid":"0000-0002-9294-6076","last_name":"Bauer","full_name":"Bauer, Matthias","id":"47241","first_name":"Matthias"},{"last_name":"Dyballa","full_name":"Dyballa, Michael","first_name":"Michael"},{"first_name":"Deven P.","last_name":"Estes","full_name":"Estes, Deven P."}],"volume":125,"citation":{"mla":"Nguyen, Hoang-Huy, et al. “Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation.” <i>The Journal of Physical Chemistry C</i>, vol. 125, no. 27, American Chemical Society (ACS), 2021, pp. 14627–35, doi:<a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">10.1021/acs.jpcc.1c02074</a>.","short":"H.-H. Nguyen, Z. Li, T. Enenkel, J. Hildebrand, M. Bauer, M. Dyballa, D.P. Estes, The Journal of Physical Chemistry C 125 (2021) 14627–14635.","bibtex":"@article{Nguyen_Li_Enenkel_Hildebrand_Bauer_Dyballa_Estes_2021, title={Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation}, volume={125}, DOI={<a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">10.1021/acs.jpcc.1c02074</a>}, number={27}, journal={The Journal of Physical Chemistry C}, publisher={American Chemical Society (ACS)}, author={Nguyen, Hoang-Huy and Li, Zheng and Enenkel, Toni and Hildebrand, Joachim and Bauer, Matthias and Dyballa, Michael and Estes, Deven P.}, year={2021}, pages={14627–14635} }","apa":"Nguyen, H.-H., Li, Z., Enenkel, T., Hildebrand, J., Bauer, M., Dyballa, M., &#38; Estes, D. P. (2021). Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation. <i>The Journal of Physical Chemistry C</i>, <i>125</i>(27), 14627–14635. <a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">https://doi.org/10.1021/acs.jpcc.1c02074</a>","chicago":"Nguyen, Hoang-Huy, Zheng Li, Toni Enenkel, Joachim Hildebrand, Matthias Bauer, Michael Dyballa, and Deven P. Estes. “Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation.” <i>The Journal of Physical Chemistry C</i> 125, no. 27 (2021): 14627–35. <a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">https://doi.org/10.1021/acs.jpcc.1c02074</a>.","ieee":"H.-H. Nguyen <i>et al.</i>, “Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation,” <i>The Journal of Physical Chemistry C</i>, vol. 125, no. 27, pp. 14627–14635, 2021, doi: <a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">10.1021/acs.jpcc.1c02074</a>.","ama":"Nguyen H-H, Li Z, Enenkel T, et al. Probing the Interactions of Immobilized Ruthenium Dihydride Complexes with Metal Oxide Surfaces by MAS NMR: Effects on CO<sub>2</sub> Hydrogenation. <i>The Journal of Physical Chemistry C</i>. 2021;125(27):14627-14635. doi:<a href=\"https://doi.org/10.1021/acs.jpcc.1c02074\">10.1021/acs.jpcc.1c02074</a>"},"intvolume":"       125","page":"14627-14635","publication_status":"published","publication_identifier":{"issn":["1932-7447","1932-7455"]},"article_type":"original","_id":"41002","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"status":"public","type":"journal_article"},{"year":"2021","citation":{"apa":"Emmerling, S. T., Ziegler, F., Fischer, F. R., Schoch, R., Bauer, M., Plietker, B., Buchmeiser, M. R., &#38; Lotsch, B. V. (2021). Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity. <i>Chemistry – A European Journal</i>, <i>28</i>(8). <a href=\"https://doi.org/10.1002/chem.202104108\">https://doi.org/10.1002/chem.202104108</a>","bibtex":"@article{Emmerling_Ziegler_Fischer_Schoch_Bauer_Plietker_Buchmeiser_Lotsch_2021, title={Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity}, volume={28}, DOI={<a href=\"https://doi.org/10.1002/chem.202104108\">10.1002/chem.202104108</a>}, number={8}, journal={Chemistry – A European Journal}, publisher={Wiley}, author={Emmerling, Sebastian T. and Ziegler, Felix and Fischer, Felix R. and Schoch, Roland and Bauer, Matthias and Plietker, Bernd and Buchmeiser, Michael R. and Lotsch, Bettina V.}, year={2021} }","short":"S.T. Emmerling, F. Ziegler, F.R. Fischer, R. Schoch, M. Bauer, B. Plietker, M.R. Buchmeiser, B.V. Lotsch, Chemistry – A European Journal 28 (2021).","mla":"Emmerling, Sebastian T., et al. “Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity.” <i>Chemistry – A European Journal</i>, vol. 28, no. 8, Wiley, 2021, doi:<a href=\"https://doi.org/10.1002/chem.202104108\">10.1002/chem.202104108</a>.","ama":"Emmerling ST, Ziegler F, Fischer FR, et al. Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity. <i>Chemistry – A European Journal</i>. 2021;28(8). doi:<a href=\"https://doi.org/10.1002/chem.202104108\">10.1002/chem.202104108</a>","chicago":"Emmerling, Sebastian T., Felix Ziegler, Felix R. Fischer, Roland Schoch, Matthias Bauer, Bernd Plietker, Michael R. Buchmeiser, and Bettina V. Lotsch. “Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity.” <i>Chemistry – A European Journal</i> 28, no. 8 (2021). <a href=\"https://doi.org/10.1002/chem.202104108\">https://doi.org/10.1002/chem.202104108</a>.","ieee":"S. T. Emmerling <i>et al.</i>, “Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity,” <i>Chemistry – A European Journal</i>, vol. 28, no. 8, 2021, doi: <a href=\"https://doi.org/10.1002/chem.202104108\">10.1002/chem.202104108</a>."},"intvolume":"        28","publication_status":"published","publication_identifier":{"issn":["0947-6539","1521-3765"]},"issue":"8","title":"Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity","doi":"10.1002/chem.202104108","date_updated":"2023-01-31T08:05:07Z","publisher":"Wiley","author":[{"full_name":"Emmerling, Sebastian T.","last_name":"Emmerling","first_name":"Sebastian T."},{"first_name":"Felix","last_name":"Ziegler","full_name":"Ziegler, Felix"},{"last_name":"Fischer","full_name":"Fischer, Felix R.","first_name":"Felix R."},{"full_name":"Schoch, Roland","id":"48467","last_name":"Schoch","orcid":"0000-0003-2061-7289","first_name":"Roland"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","full_name":"Bauer, Matthias","id":"47241"},{"last_name":"Plietker","full_name":"Plietker, Bernd","first_name":"Bernd"},{"last_name":"Buchmeiser","full_name":"Buchmeiser, Michael R.","first_name":"Michael R."},{"first_name":"Bettina V.","full_name":"Lotsch, Bettina V.","last_name":"Lotsch"}],"date_created":"2023-01-30T16:48:22Z","volume":28,"abstract":[{"text":"Covalent organic frameworks (COFs) offer vast structural and chemical diversity enabling a wide and growing range of applications. While COFs are well-established as heterogeneous catalysts, so far, their high and ordered porosity has scarcely been utilized to its full potential when it comes to spatially confined reactions in COF pores to alter the outcome of reactions. Here, we present a highly porous and crystalline, large-pore COF as catalytic support in α,ω-diene ring-closing metathesis reactions, leading to increased macrocyclization selectivity. COF pore-wall modification by immobilization of a Grubbs-Hoveyda-type catalyst via a mild silylation reaction provides a molecularly precise heterogeneous olefin metathesis catalyst. An increased macro(mono)cyclization (MMC) selectivity over oligomerization (O) for the heterogeneous COF-catalyst (MMC:O=1.35) of up to 51 % compared to the homogeneous catalyst (MMC:O=0.90) was observed along with a substrate-size dependency in selectivity, pointing to diffusion limitations induced by the pore confinement.","lang":"eng"}],"status":"public","type":"journal_article","publication":"Chemistry – A European Journal","article_type":"original","keyword":["General Chemistry","Catalysis","Organic Chemistry"],"language":[{"iso":"eng"}],"_id":"40998","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}]},{"status":"public","type":"journal_article","article_type":"original","_id":"41003","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","page":"7541-7544","intvolume":"        57","citation":{"bibtex":"@article{Reuter_Kruse_Schoch_Lochbrunner_Bauer_Heinze_2021, title={Higher MLCT lifetime of carbene iron(&#60;scp&#62;ii&#60;/scp&#62;) complexes by chelate ring expansion}, volume={57}, DOI={<a href=\"https://doi.org/10.1039/d1cc02173g\">10.1039/d1cc02173g</a>}, number={61}, journal={Chemical Communications}, publisher={Royal Society of Chemistry (RSC)}, author={Reuter, Thomas and Kruse, Ayla and Schoch, Roland and Lochbrunner, Stefan and Bauer, Matthias and Heinze, Katja}, year={2021}, pages={7541–7544} }","short":"T. Reuter, A. Kruse, R. Schoch, S. Lochbrunner, M. Bauer, K. Heinze, Chemical Communications 57 (2021) 7541–7544.","mla":"Reuter, Thomas, et al. “Higher MLCT Lifetime of Carbene Iron(&#60;scp&#62;ii&#60;/Scp&#62;) Complexes by Chelate Ring Expansion.” <i>Chemical Communications</i>, vol. 57, no. 61, Royal Society of Chemistry (RSC), 2021, pp. 7541–44, doi:<a href=\"https://doi.org/10.1039/d1cc02173g\">10.1039/d1cc02173g</a>.","apa":"Reuter, T., Kruse, A., Schoch, R., Lochbrunner, S., Bauer, M., &#38; Heinze, K. (2021). Higher MLCT lifetime of carbene iron(&#60;scp&#62;ii&#60;/scp&#62;) complexes by chelate ring expansion. <i>Chemical Communications</i>, <i>57</i>(61), 7541–7544. <a href=\"https://doi.org/10.1039/d1cc02173g\">https://doi.org/10.1039/d1cc02173g</a>","ieee":"T. Reuter, A. Kruse, R. Schoch, S. Lochbrunner, M. Bauer, and K. Heinze, “Higher MLCT lifetime of carbene iron(&#60;scp&#62;ii&#60;/scp&#62;) complexes by chelate ring expansion,” <i>Chemical Communications</i>, vol. 57, no. 61, pp. 7541–7544, 2021, doi: <a href=\"https://doi.org/10.1039/d1cc02173g\">10.1039/d1cc02173g</a>.","chicago":"Reuter, Thomas, Ayla Kruse, Roland Schoch, Stefan Lochbrunner, Matthias Bauer, and Katja Heinze. “Higher MLCT Lifetime of Carbene Iron(&#60;scp&#62;ii&#60;/Scp&#62;) Complexes by Chelate Ring Expansion.” <i>Chemical Communications</i> 57, no. 61 (2021): 7541–44. <a href=\"https://doi.org/10.1039/d1cc02173g\">https://doi.org/10.1039/d1cc02173g</a>.","ama":"Reuter T, Kruse A, Schoch R, Lochbrunner S, Bauer M, Heinze K. Higher MLCT lifetime of carbene iron(&#60;scp&#62;ii&#60;/scp&#62;) complexes by chelate ring expansion. <i>Chemical Communications</i>. 2021;57(61):7541-7544. doi:<a href=\"https://doi.org/10.1039/d1cc02173g\">10.1039/d1cc02173g</a>"},"publication_identifier":{"issn":["1359-7345","1364-548X"]},"publication_status":"published","doi":"10.1039/d1cc02173g","date_updated":"2023-01-31T08:06:16Z","volume":57,"author":[{"first_name":"Thomas","full_name":"Reuter, Thomas","last_name":"Reuter"},{"full_name":"Kruse, Ayla","last_name":"Kruse","first_name":"Ayla"},{"first_name":"Roland","id":"48467","full_name":"Schoch, Roland","orcid":"0000-0003-2061-7289","last_name":"Schoch"},{"first_name":"Stefan","full_name":"Lochbrunner, Stefan","last_name":"Lochbrunner"},{"last_name":"Bauer","orcid":"0000-0002-9294-6076","full_name":"Bauer, Matthias","id":"47241","first_name":"Matthias"},{"last_name":"Heinze","full_name":"Heinze, Katja","first_name":"Katja"}],"abstract":[{"lang":"eng","text":"Combining strong σ-donating N-heterocyclic carbene ligands and π-accepting pyridine ligands with a high octahedricity in rigid iron(II) complexes increases the 3MLCT lifetime from 0.15 ps in the prototypical [Fe(tpy)2]2+ complex to 9.2 ps in [Fe(dpmi)2]2+12+. The tripodal CNN ligand dpmi (di(pyridine-2-yl)(3-methylimidazol-2-yl)methane) forms six-membered chelate rings with the iron(II) centre leading to close to 90° bite angles and enhanced iron-ligand orbital overlap"}],"publication":"Chemical Communications","keyword":["Materials Chemistry","Metals and Alloys","Surfaces","Coatings and Films","General Chemistry","Ceramics and Composites","Electronic","Optical and Magnetic Materials","Catalysis"],"language":[{"iso":"eng"}],"year":"2021","issue":"61","title":"Higher MLCT lifetime of carbene iron(<scp>ii</scp>) complexes by chelate ring expansion","publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-30T16:49:33Z"},{"publisher":"Royal Society of Chemistry (RSC)","date_created":"2023-01-30T16:47:45Z","title":"Photoactive iron complexes: more sustainable, but still a challenge","issue":"2","year":"2021","keyword":["Inorganic Chemistry"],"language":[{"iso":"eng"}],"publication":"Inorganic Chemistry Frontiers","abstract":[{"text":"On transition metals such as iron rests lots of hope to replace precious metal catalysts in the field of photochemistry for a more sustainable future. Indeed, significant progress has been made in recent years in terms of lifetime extension and emerging applications in catalysis. For this reason, recent synthetic strategies of new photoactive iron compounds, which have proved to show particularly promising properties, are reviewed here. The lifetime of the excited state serves as a key parameter for comparison with the standard ruthenium complex, [Ru(bpy)3]2+, to discuss the potential and performance of the iron complexes. This approach is complemented by a more holistic examination of the sustainability of such a substitution strategy in order to answer the question: when or at which point can we assume that iron represents a more sustainable alternative for noble metals in photochemical applications?","lang":"eng"}],"date_updated":"2023-01-31T08:04:56Z","volume":9,"author":[{"last_name":"Dierks","full_name":"Dierks, Philipp","first_name":"Philipp"},{"full_name":"Vukadinovic, Yannik","last_name":"Vukadinovic","first_name":"Yannik"},{"first_name":"Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias"}],"doi":"10.1039/d1qi01112j","publication_identifier":{"issn":["2052-1553"]},"publication_status":"published","intvolume":"         9","page":"206-220","citation":{"mla":"Dierks, Philipp, et al. “Photoactive Iron Complexes: More Sustainable, but Still a Challenge.” <i>Inorganic Chemistry Frontiers</i>, vol. 9, no. 2, Royal Society of Chemistry (RSC), 2021, pp. 206–20, doi:<a href=\"https://doi.org/10.1039/d1qi01112j\">10.1039/d1qi01112j</a>.","short":"P. Dierks, Y. Vukadinovic, M. Bauer, Inorganic Chemistry Frontiers 9 (2021) 206–220.","bibtex":"@article{Dierks_Vukadinovic_Bauer_2021, title={Photoactive iron complexes: more sustainable, but still a challenge}, volume={9}, DOI={<a href=\"https://doi.org/10.1039/d1qi01112j\">10.1039/d1qi01112j</a>}, number={2}, journal={Inorganic Chemistry Frontiers}, publisher={Royal Society of Chemistry (RSC)}, author={Dierks, Philipp and Vukadinovic, Yannik and Bauer, Matthias}, year={2021}, pages={206–220} }","apa":"Dierks, P., Vukadinovic, Y., &#38; Bauer, M. (2021). Photoactive iron complexes: more sustainable, but still a challenge. <i>Inorganic Chemistry Frontiers</i>, <i>9</i>(2), 206–220. <a href=\"https://doi.org/10.1039/d1qi01112j\">https://doi.org/10.1039/d1qi01112j</a>","ama":"Dierks P, Vukadinovic Y, Bauer M. Photoactive iron complexes: more sustainable, but still a challenge. <i>Inorganic Chemistry Frontiers</i>. 2021;9(2):206-220. doi:<a href=\"https://doi.org/10.1039/d1qi01112j\">10.1039/d1qi01112j</a>","chicago":"Dierks, Philipp, Yannik Vukadinovic, and Matthias Bauer. “Photoactive Iron Complexes: More Sustainable, but Still a Challenge.” <i>Inorganic Chemistry Frontiers</i> 9, no. 2 (2021): 206–20. <a href=\"https://doi.org/10.1039/d1qi01112j\">https://doi.org/10.1039/d1qi01112j</a>.","ieee":"P. Dierks, Y. Vukadinovic, and M. Bauer, “Photoactive iron complexes: more sustainable, but still a challenge,” <i>Inorganic Chemistry Frontiers</i>, vol. 9, no. 2, pp. 206–220, 2021, doi: <a href=\"https://doi.org/10.1039/d1qi01112j\">10.1039/d1qi01112j</a>."},"_id":"40997","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","article_type":"review","type":"journal_article","status":"public"},{"_id":"41000","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"article_type":"original","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"type":"journal_article","publication":"Angewandte Chemie International Edition","abstract":[{"lang":"eng","text":"Metal-catalyzed C−H activations are environmentally and economically attractive synthetic strategies for the construction of functional molecules as they obviate the need for pre-functionalized substrates and minimize waste generation. Great challenges reside in the control of selectivities, the utilization of unbiased hydrocarbons, and the operation of atom-economical dehydrocoupling mechanisms. An especially mild borylation of benzylic CH bonds was developed with the ligand-free pre-catalyst Co[N(SiMe3)2]2 and the bench-stable and inexpensive borylation reagent B2pin2 that produces H2 as the only by-product. A full set of kinetic, spectroscopic, and preparative mechanistic studies are indicative of a tandem catalysis mechanism of CH-borylation and dehydrocoupling via molecular CoI catalysts."}],"status":"public","publisher":"Wiley","date_updated":"2023-01-31T08:05:26Z","author":[{"first_name":"Pradip","full_name":"Ghosh, Pradip","last_name":"Ghosh"},{"orcid":"0000-0003-2061-7289","last_name":"Schoch","full_name":"Schoch, Roland","id":"48467","first_name":"Roland"},{"last_name":"Bauer","orcid":"0000-0002-9294-6076","id":"47241","full_name":"Bauer, Matthias","first_name":"Matthias"},{"full_name":"Jacobi von Wangelin, Axel","last_name":"Jacobi von Wangelin","first_name":"Axel"}],"date_created":"2023-01-30T16:48:53Z","volume":61,"title":"Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis","doi":"10.1002/anie.202110821","publication_status":"published","publication_identifier":{"issn":["1433-7851","1521-3773"]},"issue":"1","year":"2021","citation":{"apa":"Ghosh, P., Schoch, R., Bauer, M., &#38; Jacobi von Wangelin, A. (2021). Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis. <i>Angewandte Chemie International Edition</i>, <i>61</i>(1). <a href=\"https://doi.org/10.1002/anie.202110821\">https://doi.org/10.1002/anie.202110821</a>","short":"P. Ghosh, R. Schoch, M. Bauer, A. Jacobi von Wangelin, Angewandte Chemie International Edition 61 (2021).","mla":"Ghosh, Pradip, et al. “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis.” <i>Angewandte Chemie International Edition</i>, vol. 61, no. 1, Wiley, 2021, doi:<a href=\"https://doi.org/10.1002/anie.202110821\">10.1002/anie.202110821</a>.","bibtex":"@article{Ghosh_Schoch_Bauer_Jacobi von Wangelin_2021, title={Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis}, volume={61}, DOI={<a href=\"https://doi.org/10.1002/anie.202110821\">10.1002/anie.202110821</a>}, number={1}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Ghosh, Pradip and Schoch, Roland and Bauer, Matthias and Jacobi von Wangelin, Axel}, year={2021} }","ama":"Ghosh P, Schoch R, Bauer M, Jacobi von Wangelin A. Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis. <i>Angewandte Chemie International Edition</i>. 2021;61(1). doi:<a href=\"https://doi.org/10.1002/anie.202110821\">10.1002/anie.202110821</a>","ieee":"P. Ghosh, R. Schoch, M. Bauer, and A. Jacobi von Wangelin, “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis,” <i>Angewandte Chemie International Edition</i>, vol. 61, no. 1, 2021, doi: <a href=\"https://doi.org/10.1002/anie.202110821\">10.1002/anie.202110821</a>.","chicago":"Ghosh, Pradip, Roland Schoch, Matthias Bauer, and Axel Jacobi von Wangelin. “Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis.” <i>Angewandte Chemie International Edition</i> 61, no. 1 (2021). <a href=\"https://doi.org/10.1002/anie.202110821\">https://doi.org/10.1002/anie.202110821</a>."},"intvolume":"        61"},{"keyword":["Materials Chemistry","General Chemical Engineering","General Chemistry"],"language":[{"iso":"eng"}],"publication":"Chemistry of Materials","abstract":[{"text":"Within this article, it is shown that an electrochemical defluorination and additional fluorination of Ruddlesden–Popper-type La2NiO3F2 is possible within all-solid-state fluoride-ion batteries. Structural changes within the reduced and oxidized phases have been examined by X-ray diffraction studies at different states of charging and discharging. The synthesis of the oxidized phase La2NiO3F2+x proved to be successful by structural analysis using both X-ray powder diffraction and automated electron diffraction tomography techniques. The structural reversibility on re-fluorinating and re-defluorinating is also demonstrated. Moreover, the influence of different sequences of consecutive reduction and oxidation steps on the formed phases has been investigated. The observed structural changes have been compared to changes in phases obtained via other topochemical modification approaches such as hydride-based reduction and oxidative fluorination using F2 gas, highlighting the potential of such electrochemical reactions as alternative synthesis routes. Furthermore, the electrochemical routes represent safe and controllable synthesis approaches for novel phases, which cannot be synthesized via other topochemical methods. Additionally, side reactions, occurring alongside the desired electrochemical reactions, have been addressed and the cycling performance has been studied.","lang":"eng"}],"publisher":"American Chemical Society (ACS)","date_created":"2023-01-30T17:01:00Z","title":"Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries","issue":"2","year":"2021","_id":"41013","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","article_type":"original","type":"journal_article","status":"public","date_updated":"2023-01-31T08:07:28Z","volume":33,"author":[{"full_name":"Wissel, Kerstin","last_name":"Wissel","first_name":"Kerstin"},{"first_name":"Roland","last_name":"Schoch","orcid":"0000-0003-2061-7289","id":"48467","full_name":"Schoch, Roland"},{"full_name":"Vogel, Tobias","last_name":"Vogel","first_name":"Tobias"},{"first_name":"Manuel","full_name":"Donzelli, Manuel","last_name":"Donzelli"},{"first_name":"Galina","full_name":"Matveeva, Galina","last_name":"Matveeva"},{"first_name":"Ute","full_name":"Kolb, Ute","last_name":"Kolb"},{"orcid":"0000-0002-9294-6076","last_name":"Bauer","id":"47241","full_name":"Bauer, Matthias","first_name":"Matthias"},{"first_name":"Peter R.","full_name":"Slater, Peter R.","last_name":"Slater"},{"last_name":"Clemens","full_name":"Clemens, Oliver","first_name":"Oliver"}],"doi":"10.1021/acs.chemmater.0c01762","publication_identifier":{"issn":["0897-4756","1520-5002"]},"publication_status":"published","page":"499-512","intvolume":"        33","citation":{"short":"K. Wissel, R. Schoch, T. Vogel, M. Donzelli, G. Matveeva, U. Kolb, M. Bauer, P.R. Slater, O. Clemens, Chemistry of Materials 33 (2021) 499–512.","mla":"Wissel, Kerstin, et al. “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries.” <i>Chemistry of Materials</i>, vol. 33, no. 2, American Chemical Society (ACS), 2021, pp. 499–512, doi:<a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">10.1021/acs.chemmater.0c01762</a>.","bibtex":"@article{Wissel_Schoch_Vogel_Donzelli_Matveeva_Kolb_Bauer_Slater_Clemens_2021, title={Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries}, volume={33}, DOI={<a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">10.1021/acs.chemmater.0c01762</a>}, number={2}, journal={Chemistry of Materials}, publisher={American Chemical Society (ACS)}, author={Wissel, Kerstin and Schoch, Roland and Vogel, Tobias and Donzelli, Manuel and Matveeva, Galina and Kolb, Ute and Bauer, Matthias and Slater, Peter R. and Clemens, Oliver}, year={2021}, pages={499–512} }","apa":"Wissel, K., Schoch, R., Vogel, T., Donzelli, M., Matveeva, G., Kolb, U., Bauer, M., Slater, P. R., &#38; Clemens, O. (2021). Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries. <i>Chemistry of Materials</i>, <i>33</i>(2), 499–512. <a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">https://doi.org/10.1021/acs.chemmater.0c01762</a>","ieee":"K. Wissel <i>et al.</i>, “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries,” <i>Chemistry of Materials</i>, vol. 33, no. 2, pp. 499–512, 2021, doi: <a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">10.1021/acs.chemmater.0c01762</a>.","chicago":"Wissel, Kerstin, Roland Schoch, Tobias Vogel, Manuel Donzelli, Galina Matveeva, Ute Kolb, Matthias Bauer, Peter R. Slater, and Oliver Clemens. “Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries.” <i>Chemistry of Materials</i> 33, no. 2 (2021): 499–512. <a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">https://doi.org/10.1021/acs.chemmater.0c01762</a>.","ama":"Wissel K, Schoch R, Vogel T, et al. Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La<sub>2</sub>NiO<sub>3</sub>F<sub>2</sub> within Fluoride-Ion Batteries. <i>Chemistry of Materials</i>. 2021;33(2):499-512. doi:<a href=\"https://doi.org/10.1021/acs.chemmater.0c01762\">10.1021/acs.chemmater.0c01762</a>"}},{"status":"public","type":"journal_article","article_type":"original","_id":"41010","department":[{"_id":"35"},{"_id":"306"}],"user_id":"48467","intvolume":"        60","page":"9534-9539","citation":{"apa":"Watt, F. A., Burkhardt, L., Schoch, R., Mitzinger, S., Bauer, M., Weigend, F., Goicoechea, J. M., Tambornino, F., &#38; Hohloch, S. (2021). η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**. <i>Angewandte Chemie International Edition</i>, <i>60</i>(17), 9534–9539. <a href=\"https://doi.org/10.1002/anie.202100559\">https://doi.org/10.1002/anie.202100559</a>","bibtex":"@article{Watt_Burkhardt_Schoch_Mitzinger_Bauer_Weigend_Goicoechea_Tambornino_Hohloch_2021, title={η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**}, volume={60}, DOI={<a href=\"https://doi.org/10.1002/anie.202100559\">10.1002/anie.202100559</a>}, number={17}, journal={Angewandte Chemie International Edition}, publisher={Wiley}, author={Watt, Fabian A. and Burkhardt, Lukas and Schoch, Roland and Mitzinger, Stefan and Bauer, Matthias and Weigend, Florian and Goicoechea, Jose M. and Tambornino, Frank and Hohloch, Stephan}, year={2021}, pages={9534–9539} }","short":"F.A. Watt, L. Burkhardt, R. Schoch, S. Mitzinger, M. Bauer, F. Weigend, J.M. Goicoechea, F. Tambornino, S. Hohloch, Angewandte Chemie International Edition 60 (2021) 9534–9539.","mla":"Watt, Fabian A., et al. “η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**.” <i>Angewandte Chemie International Edition</i>, vol. 60, no. 17, Wiley, 2021, pp. 9534–39, doi:<a href=\"https://doi.org/10.1002/anie.202100559\">10.1002/anie.202100559</a>.","ama":"Watt FA, Burkhardt L, Schoch R, et al. η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**. <i>Angewandte Chemie International Edition</i>. 2021;60(17):9534-9539. doi:<a href=\"https://doi.org/10.1002/anie.202100559\">10.1002/anie.202100559</a>","ieee":"F. A. Watt <i>et al.</i>, “η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**,” <i>Angewandte Chemie International Edition</i>, vol. 60, no. 17, pp. 9534–9539, 2021, doi: <a href=\"https://doi.org/10.1002/anie.202100559\">10.1002/anie.202100559</a>.","chicago":"Watt, Fabian A., Lukas Burkhardt, Roland Schoch, Stefan Mitzinger, Matthias Bauer, Florian Weigend, Jose M. Goicoechea, Frank Tambornino, and Stephan Hohloch. “η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**.” <i>Angewandte Chemie International Edition</i> 60, no. 17 (2021): 9534–39. <a href=\"https://doi.org/10.1002/anie.202100559\">https://doi.org/10.1002/anie.202100559</a>."},"publication_identifier":{"issn":["1433-7851","1521-3773"]},"publication_status":"published","doi":"10.1002/anie.202100559","date_updated":"2023-01-31T08:06:50Z","volume":60,"author":[{"full_name":"Watt, Fabian A.","last_name":"Watt","first_name":"Fabian A."},{"full_name":"Burkhardt, Lukas","last_name":"Burkhardt","first_name":"Lukas"},{"last_name":"Schoch","orcid":"0000-0003-2061-7289","id":"48467","full_name":"Schoch, Roland","first_name":"Roland"},{"first_name":"Stefan","full_name":"Mitzinger, Stefan","last_name":"Mitzinger"},{"first_name":"Matthias","id":"47241","full_name":"Bauer, Matthias","last_name":"Bauer","orcid":"0000-0002-9294-6076"},{"last_name":"Weigend","full_name":"Weigend, Florian","first_name":"Florian"},{"first_name":"Jose M.","last_name":"Goicoechea","full_name":"Goicoechea, Jose M."},{"full_name":"Tambornino, Frank","last_name":"Tambornino","first_name":"Frank"},{"full_name":"Hohloch, Stephan","last_name":"Hohloch","first_name":"Stephan"}],"abstract":[{"lang":"eng","text":"We present the η3-coordination of the 2-phosphaethynthiolate anion in the complex (PN)2La(SCP) (2) [PN=N-(2-(diisopropylphosphanyl)-4-methylphenyl)-2,4,6-trimethylanilide)]. Structural comparison with dinuclear thiocyanate-bridged (PN)2La(μ-1,3-SCN)2La(PN)2 (3) and azide-bridged (PN)2La(μ-1,3-N3)2La(PN)2 (4) complexes indicates that the [SCP]− coordination mode is mainly governed by electronic, rather than steric factors. Quantum mechanical investigations reveal large contributions of the antibonding π*-orbital of the [SCP]− ligand to the LUMO of complex 2, rendering it the ideal precursor for the first functionalization of the [SCP]− anion. Complex 2 was therefore reacted with CAACs which induced a selective rearrangement of the [SCP]− ligand to form the first CAAC stabilized group 15–group 16 fulminate-type complexes (PN)2La{SPC(RCAAC)} (5 a,b, R=Ad, Me). A detailed reaction mechanism for the SCP-to-SPC isomerization is proposed based on DFT calculations."}],"publication":"Angewandte Chemie International Edition","keyword":["General Chemistry","Catalysis"],"language":[{"iso":"eng"}],"year":"2021","issue":"17","title":"η            <sup>3</sup>            ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**","publisher":"Wiley","date_created":"2023-01-30T17:00:21Z"},{"doi":"10.1021/acs.inorgchem.0c03259","date_updated":"2023-01-31T08:07:16Z","author":[{"first_name":"Mario","last_name":"Winkler","full_name":"Winkler, Mario"},{"full_name":"Schnierle, Marc","last_name":"Schnierle","first_name":"Marc"},{"first_name":"Felix","full_name":"Ehrlich, Felix","last_name":"Ehrlich"},{"first_name":"Kim-Isabelle","full_name":"Mehnert, Kim-Isabelle","last_name":"Mehnert"},{"last_name":"Hunger","full_name":"Hunger, David","first_name":"David"},{"first_name":"Alena M.","last_name":"Sheveleva","full_name":"Sheveleva, Alena M."},{"full_name":"Burkhardt, Lukas","last_name":"Burkhardt","first_name":"Lukas"},{"first_name":"Matthias","id":"47241","full_name":"Bauer, Matthias","orcid":"0000-0002-9294-6076","last_name":"Bauer"},{"first_name":"Floriana","full_name":"Tuna, Floriana","last_name":"Tuna"},{"first_name":"Mark R.","full_name":"Ringenberg, Mark R.","last_name":"Ringenberg"},{"full_name":"van Slageren, Joris","last_name":"van Slageren","first_name":"Joris"}],"volume":60,"citation":{"mla":"Winkler, Mario, et al. “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(Dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>.” <i>Inorganic Chemistry</i>, vol. 60, no. 5, American Chemical Society (ACS), 2021, pp. 2856–65, doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">10.1021/acs.inorgchem.0c03259</a>.","bibtex":"@article{Winkler_Schnierle_Ehrlich_Mehnert_Hunger_Sheveleva_Burkhardt_Bauer_Tuna_Ringenberg_et al._2021, title={Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>}, volume={60}, DOI={<a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">10.1021/acs.inorgchem.0c03259</a>}, number={5}, journal={Inorganic Chemistry}, publisher={American Chemical Society (ACS)}, author={Winkler, Mario and Schnierle, Marc and Ehrlich, Felix and Mehnert, Kim-Isabelle and Hunger, David and Sheveleva, Alena M. and Burkhardt, Lukas and Bauer, Matthias and Tuna, Floriana and Ringenberg, Mark R. and et al.}, year={2021}, pages={2856–2865} }","short":"M. Winkler, M. Schnierle, F. Ehrlich, K.-I. Mehnert, D. Hunger, A.M. Sheveleva, L. Burkhardt, M. Bauer, F. Tuna, M.R. Ringenberg, J. van Slageren, Inorganic Chemistry 60 (2021) 2856–2865.","apa":"Winkler, M., Schnierle, M., Ehrlich, F., Mehnert, K.-I., Hunger, D., Sheveleva, A. M., Burkhardt, L., Bauer, M., Tuna, F., Ringenberg, M. R., &#38; van Slageren, J. (2021). Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>. <i>Inorganic Chemistry</i>, <i>60</i>(5), 2856–2865. <a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">https://doi.org/10.1021/acs.inorgchem.0c03259</a>","ama":"Winkler M, Schnierle M, Ehrlich F, et al. Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>. <i>Inorganic Chemistry</i>. 2021;60(5):2856-2865. doi:<a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">10.1021/acs.inorgchem.0c03259</a>","ieee":"M. Winkler <i>et al.</i>, “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>,” <i>Inorganic Chemistry</i>, vol. 60, no. 5, pp. 2856–2865, 2021, doi: <a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">10.1021/acs.inorgchem.0c03259</a>.","chicago":"Winkler, Mario, Marc Schnierle, Felix Ehrlich, Kim-Isabelle Mehnert, David Hunger, Alena M. Sheveleva, Lukas Burkhardt, et al. “Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(Dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>.” <i>Inorganic Chemistry</i> 60, no. 5 (2021): 2856–65. <a href=\"https://doi.org/10.1021/acs.inorgchem.0c03259\">https://doi.org/10.1021/acs.inorgchem.0c03259</a>."},"intvolume":"        60","page":"2856-2865","publication_status":"published","publication_identifier":{"issn":["0020-1669","1520-510X"]},"article_type":"original","_id":"41012","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"status":"public","type":"journal_article","title":"Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) <sub>3</sub>]<sup>+/0</sup>","publisher":"American Chemical Society (ACS)","date_created":"2023-01-30T17:00:49Z","year":"2021","issue":"5","keyword":["Inorganic Chemistry","Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"abstract":[{"text":"Here we explore the electronic structure of the diiron complex [(dppf)Fe(CO)3]0/+ [10/+; dppf = 1,1′-bis(diphenylphosphino)ferrocene] in two oxidation states by an advanced multitechnique experimental approach. A combination of magnetic circular dichroism, X-ray absorption and emission, high-frequency electron paramagnetic resonance (EPR), and Mössbauer spectroscopies is used to establish that oxidation of 10 occurs on the carbonyl iron ion, resulting in a low-spin iron(I) ion. It is shown that an unequivocal result is obtained by combining several methods. Compound 1+ displays slow spin dynamics, which is used here to study its geometric structure by means of pulsed EPR methods. Surprisingly, these data show an association of the tetrakis[3,5-bis(trifluoromethylphenyl)]borate counterion with 1+.","lang":"eng"}],"publication":"Inorganic Chemistry"},{"title":"Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles","date_created":"2023-01-30T17:00:36Z","publisher":"Wiley","year":"2021","issue":"2","language":[{"iso":"eng"}],"keyword":["General Chemistry"],"abstract":[{"text":"The controlled assembly of well-defined planar nanoclusters from molecular precursors is synthetically challenging and often plagued by the predominant formation of 3D-structures and nanoparticles. Herein, we report planar iron hydride nanoclusters from reactions of main group element hydrides with iron(II) bis(hexamethyldisilazide). The structures and properties of isolated Fe4, Fe6, and Fe7 nanoplatelets and calculated intermediates enable an unprecedented insight into the underlying building principle and growth mechanism of iron clusters, metal monolayers, and nanoparticles.","lang":"eng"}],"publication":"ChemistryOpen","doi":"10.1002/open.202000307","author":[{"first_name":"Uttam","full_name":"Chakraborty, Uttam","last_name":"Chakraborty"},{"last_name":"Bügel","full_name":"Bügel, Patrick","first_name":"Patrick"},{"full_name":"Fritsch, Lorena","id":"44418","last_name":"Fritsch","first_name":"Lorena"},{"first_name":"Florian","last_name":"Weigend","full_name":"Weigend, Florian"},{"last_name":"Bauer","orcid":"0000-0002-9294-6076","full_name":"Bauer, Matthias","id":"47241","first_name":"Matthias"},{"full_name":"Jacobi von Wangelin, Axel","last_name":"Jacobi von Wangelin","first_name":"Axel"}],"volume":10,"date_updated":"2023-01-31T08:07:01Z","citation":{"apa":"Chakraborty, U., Bügel, P., Fritsch, L., Weigend, F., Bauer, M., &#38; Jacobi von Wangelin, A. (2021). Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles. <i>ChemistryOpen</i>, <i>10</i>(2), 265–271. <a href=\"https://doi.org/10.1002/open.202000307\">https://doi.org/10.1002/open.202000307</a>","bibtex":"@article{Chakraborty_Bügel_Fritsch_Weigend_Bauer_Jacobi von Wangelin_2021, title={Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles}, volume={10}, DOI={<a href=\"https://doi.org/10.1002/open.202000307\">10.1002/open.202000307</a>}, number={2}, journal={ChemistryOpen}, publisher={Wiley}, author={Chakraborty, Uttam and Bügel, Patrick and Fritsch, Lorena and Weigend, Florian and Bauer, Matthias and Jacobi von Wangelin, Axel}, year={2021}, pages={265–271} }","mla":"Chakraborty, Uttam, et al. “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles.” <i>ChemistryOpen</i>, vol. 10, no. 2, Wiley, 2021, pp. 265–71, doi:<a href=\"https://doi.org/10.1002/open.202000307\">10.1002/open.202000307</a>.","short":"U. Chakraborty, P. Bügel, L. Fritsch, F. Weigend, M. Bauer, A. Jacobi von Wangelin, ChemistryOpen 10 (2021) 265–271.","ama":"Chakraborty U, Bügel P, Fritsch L, Weigend F, Bauer M, Jacobi von Wangelin A. Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles. <i>ChemistryOpen</i>. 2021;10(2):265-271. doi:<a href=\"https://doi.org/10.1002/open.202000307\">10.1002/open.202000307</a>","ieee":"U. Chakraborty, P. Bügel, L. Fritsch, F. Weigend, M. Bauer, and A. Jacobi von Wangelin, “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles,” <i>ChemistryOpen</i>, vol. 10, no. 2, pp. 265–271, 2021, doi: <a href=\"https://doi.org/10.1002/open.202000307\">10.1002/open.202000307</a>.","chicago":"Chakraborty, Uttam, Patrick Bügel, Lorena Fritsch, Florian Weigend, Matthias Bauer, and Axel Jacobi von Wangelin. “Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles.” <i>ChemistryOpen</i> 10, no. 2 (2021): 265–71. <a href=\"https://doi.org/10.1002/open.202000307\">https://doi.org/10.1002/open.202000307</a>."},"intvolume":"        10","page":"265-271","publication_status":"published","publication_identifier":{"issn":["2191-1363","2191-1363"]},"article_type":"original","user_id":"48467","department":[{"_id":"35"},{"_id":"306"}],"_id":"41011","status":"public","type":"journal_article"},{"status":"public","type":"journal_article","publication":"The Journal of Physical Chemistry A","keyword":["Physical and Theoretical Chemistry"],"language":[{"iso":"eng"}],"_id":"41326","user_id":"78878","year":"2021","citation":{"ieee":"K. Wojtaszek <i>et al.</i>, “Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium,” <i>The Journal of Physical Chemistry A</i>, vol. 125, no. 1, pp. 50–56, 2021, doi: <a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">10.1021/acs.jpca.0c07955</a>.","chicago":"Wojtaszek, Klaudia, Wojciech Błachucki, Krzysztof Tyrała, Michał Nowakowski, Marcin Zaja̧c, Joanna Stȩpień, Paweł Jagodziński, et al. “Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium.” <i>The Journal of Physical Chemistry A</i> 125, no. 1 (2021): 50–56. <a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">https://doi.org/10.1021/acs.jpca.0c07955</a>.","ama":"Wojtaszek K, Błachucki W, Tyrała K, et al. Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium. <i>The Journal of Physical Chemistry A</i>. 2021;125(1):50-56. doi:<a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">10.1021/acs.jpca.0c07955</a>","short":"K. Wojtaszek, W. Błachucki, K. Tyrała, M. Nowakowski, M. Zaja̧c, J. Stȩpień, P. Jagodziński, D. Banaś, W. Stańczyk, J. Czapla-Masztafiak, W.M. Kwiatek, J. Szlachetko, A. Wach, The Journal of Physical Chemistry A 125 (2021) 50–56.","bibtex":"@article{Wojtaszek_Błachucki_Tyrała_Nowakowski_Zaja̧c_Stȩpień_Jagodziński_Banaś_Stańczyk_Czapla-Masztafiak_et al._2021, title={Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium}, volume={125}, DOI={<a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">10.1021/acs.jpca.0c07955</a>}, number={1}, journal={The Journal of Physical Chemistry A}, publisher={American Chemical Society (ACS)}, author={Wojtaszek, Klaudia and Błachucki, Wojciech and Tyrała, Krzysztof and Nowakowski, Michał and Zaja̧c, Marcin and Stȩpień, Joanna and Jagodziński, Paweł and Banaś, Dariusz and Stańczyk, Wiktoria and Czapla-Masztafiak, Joanna and et al.}, year={2021}, pages={50–56} }","mla":"Wojtaszek, Klaudia, et al. “Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium.” <i>The Journal of Physical Chemistry A</i>, vol. 125, no. 1, American Chemical Society (ACS), 2021, pp. 50–56, doi:<a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">10.1021/acs.jpca.0c07955</a>.","apa":"Wojtaszek, K., Błachucki, W., Tyrała, K., Nowakowski, M., Zaja̧c, M., Stȩpień, J., Jagodziński, P., Banaś, D., Stańczyk, W., Czapla-Masztafiak, J., Kwiatek, W. M., Szlachetko, J., &#38; Wach, A. (2021). Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium. <i>The Journal of Physical Chemistry A</i>, <i>125</i>(1), 50–56. <a href=\"https://doi.org/10.1021/acs.jpca.0c07955\">https://doi.org/10.1021/acs.jpca.0c07955</a>"},"page":"50-56","intvolume":"       125","publication_status":"published","publication_identifier":{"issn":["1089-5639","1520-5215"]},"issue":"1","title":"Determination of Crystal-Field Splitting Induced by Thermal Oxidation of Titanium","doi":"10.1021/acs.jpca.0c07955","publisher":"American Chemical Society (ACS)","date_updated":"2023-02-01T08:50:50Z","date_created":"2023-01-31T22:51:45Z","author":[{"full_name":"Wojtaszek, Klaudia","last_name":"Wojtaszek","first_name":"Klaudia"},{"first_name":"Wojciech","last_name":"Błachucki","full_name":"Błachucki, Wojciech"},{"first_name":"Krzysztof","full_name":"Tyrała, Krzysztof","last_name":"Tyrała"},{"last_name":"Nowakowski","full_name":"Nowakowski, Michał","first_name":"Michał"},{"first_name":"Marcin","full_name":"Zaja̧c, Marcin","last_name":"Zaja̧c"},{"full_name":"Stȩpień, Joanna","last_name":"Stȩpień","first_name":"Joanna"},{"first_name":"Paweł","last_name":"Jagodziński","full_name":"Jagodziński, Paweł"},{"first_name":"Dariusz","full_name":"Banaś, Dariusz","last_name":"Banaś"},{"first_name":"Wiktoria","last_name":"Stańczyk","full_name":"Stańczyk, Wiktoria"},{"last_name":"Czapla-Masztafiak","full_name":"Czapla-Masztafiak, Joanna","first_name":"Joanna"},{"last_name":"Kwiatek","full_name":"Kwiatek, Wojciech M.","first_name":"Wojciech M."},{"first_name":"Jakub","last_name":"Szlachetko","full_name":"Szlachetko, Jakub"},{"first_name":"Anna","last_name":"Wach","full_name":"Wach, Anna"}],"volume":125}]